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Respiratory disease affects respiratory organs such as nasal cavity, pharynx, larynx, trachea, bronchus, lung, thorax, diaphragm. Typical respiratory infections include colds and influenza, bronchitis, and pneumonia.
FDA EUA Approved KOREA MFDS Approved STANDARD M nCoV Real-Time Detection kit is used for rapid identification and detection of novel coronavirus (2019-nCoV) nucleic acids in human nasopharyngeal swabs and throat swab samples.
WHO EUL KOREA MFDS ApprovedTGA Approved STANDARD Q COVID-19 Ag Test is a rapid chromatographic immunoassay for the qualitative detection of specific antigens to SARS-CoV-2 present in human nasopharynx.
KOREA MFDS Approved STANDARD Q COVID-19 IgM/IgG Plus Test kit is a rapid chromatographic immunoassay for the qualitative presumptive detection of specific IgM and IgG to 2019 novel coronavirus (nCoV) in humoral fluid.
STANDARD Q COVID-19 IgM/IgG Combo Test Kit is a rapid immunochromatography test designed for the qualitative presumptive detection of specific IgM and IgG to SARS-CoV-2 in humoral fluid.
STANDARD Q COVID-19 IgM/IgG Duo Test Kit is a rapid immunochromatography test designed for the qualitative presumptive detection of specific IgM and IgG to SARS-CoV-2 in humoral fluid.
STANDARD F COVID-19 Ag FIA is the fluorescent immunoassay to detect SARS-CoV-2 infection in human nasopharyngeal swab specimen, identifying existence of SARS-CoV-2 viral nucleoprotein antigens.
STANDARD F COVID-19 IgM/IgG Combo FIA is the fluorescent immunoassay to detect the qualitative presumptive detection of specific IgM and IgG to 2019 novel coronavirus (nCoV) in humoral fluid.
The STANDARD M Flu/SARS-CoV-2 Real-Time Detection Kit allows for ongoing flu surveillance while also testing for SARS-CoV-2 using Multiplex Real-Time RT PCR assay.
This product performs qualitative analysis by detecting influenza virus A type and B type antigens in the nasopharyngeal sample.
This product performs qualitative analysis by detecting RSV antigens in the nasopharyngeal sample.
This product performs qualitative analysis by detecting Group A streptococcal antigens in samples.
This product performs qualitative analysis by detecting Group A streptococcal antigens.
This product performs qualitative analysis by detecting Legionella Pneumophila antigens in the urine samples.
This product performs qualitative analysis by detecting Legionella pnemophila antigens in urine.
This product performs qualitative analysis by detecting Streptococcus pneumoniae antigens in urine samples.
This product performs qualitative analysis by detectiong Streptococcus pneumoniae antigen in urine.
STANDARD F Adeno Respi FIA test (Analyzer+Test device) is a rapid diagnostic test that can use commercially.
STANDARD Q Adeno Respi Ag Test is an immunoassay that can identify the presence of Adenovirus antigens in respiratory specimens.
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